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黑色素瘤中与免疫检查点抑制剂相关的结节病样肉芽肿病

Sarcoid-like Granulomatosis Associated with Immune Checkpoint Inhibitors in Melanoma.

作者信息

Melin Audrey, Routier Émilie, Roy Séverine, Pradere Pauline, Le Pavec Jerome, Pierre Thibaut, Chanson Noémie, Scoazec Jean-Yves, Lambotte Olivier, Robert Caroline

机构信息

Department of Dermatology, Gustave Roussy, 114 rue Edouard-Vaillant, 94800 Villejuif, France.

Service de Pneumologie et Transplantation Pulmonaire, Hôpital Marie-Lannelongue, Groupe Hospitalier Paris-Saint Joseph, 133 Av. de la Résistance, 92350 Le Plessis-Robinson, France.

出版信息

Cancers (Basel). 2022 Jun 14;14(12):2937. doi: 10.3390/cancers14122937.

Abstract

We aimed to review the clinical and biological presentation of granulomatosis associated with immune-checkpoint inhibitors (ICI) in patients with melanoma and to explore its association with classical sarcoidosis as well as with cancer response to ICI. To this end, a retrospective study on 18 melanoma patients with histologically proven ICI-induced granulomatosis over a 12-year period in a single center, as well as on 67 similar cases reported in the literature, was conducted. Results indicate ICI-induced granulomatosis is an early side effect (median time to onset: 2 months). Its clinical presentation, with predominant (90%) thoracic involvement, histopathological appearance and supposed underlying biology (involving the mTOR pathway in immune cells, Th17 polarization and TReg dysfunction) are indistinguishable from those of sarcoidosis. Moreover, it appears to be associated with ICI benefit (>65% objective response rate). Evolution is generally favorable, and symptomatic steroid treatment and/or ICI discontinuation are rarely necessary. ICI-associated granulomatosis is critical to explore for several reasons. Practically, it is essential to differentiate it from cancer progression. Secondly, this “experimental” sarcoidosis brings new elements that may help to address sarcoidosis origin and pathophysiology. Its association with ICI efficacy must be confirmed on a larger scale but could have significant impacts on patient management and biomarker definition.

摘要

我们旨在回顾黑色素瘤患者中与免疫检查点抑制剂(ICI)相关的肉芽肿病的临床和生物学表现,并探讨其与经典结节病以及癌症对ICI反应的关联。为此,我们对单中心12年间18例经组织学证实为ICI诱导的肉芽肿病的黑色素瘤患者以及文献报道的67例类似病例进行了回顾性研究。结果表明,ICI诱导的肉芽肿病是一种早期副作用(中位发病时间:2个月)。其临床表现以胸部受累为主(90%),组织病理学表现及推测的潜在生物学机制(涉及免疫细胞中的mTOR通路、Th17极化和调节性T细胞功能障碍)与结节病难以区分。此外,它似乎与ICI疗效相关(客观缓解率>65%)。病情进展通常良好,很少需要进行有症状的类固醇治疗和/或停用ICI。ICI相关的肉芽肿病因其多种原因而值得深入研究。实际上,将其与癌症进展区分开来至关重要。其次,这种“实验性”结节病带来了新的因素,可能有助于探究结节病的起源和病理生理学。其与ICI疗效的关联必须在更大规模上得到证实,但可能会对患者管理和生物标志物定义产生重大影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1837/9221061/1f06d56dc33b/cancers-14-02937-g001.jpg

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